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GM23243 LCL from B-Lymphocyte

Description:

MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD
DYSTROPHIN; DMD

Affected:

Yes

Sex:

Male

Age:

No Data

  • Overview
  • Characterizations
  • Phenotypic Data
  • External Links
  • Culture Protocols

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Muscular Dystrophies
Class Congenital Muscle Diseases
Biopsy Source Peripheral vein
Cell Type B-Lymphocyte
Tissue Type Blood
Transformant Epstein-Barr Virus
Sample Source LCL from B-Lymphocyte
Family Member 1
Family History N
Relation to Proband proband
Confirmation Molecular characterization before cell line submission to CCR
Species Homo sapiens
Common Name Human
Remarks Clinically affected; affected brother is GM23244; delayed motor development; frequent falls; diagnosed at 8 years of age; walks without assistance; currently on daily corticosteroids; also on Enalapril; donor subject has a duplication of exons 3-44 in the DMD gene

Characterizations

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IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin Confirmed by LINE assay
 
Gene DMD
Chromosomal Location Xp21.2
Allelic Variant 1 ; DUCHENNE MUSCULAR DYSTROPHY
Identified Mutation EX3-44dup

Phenotypic Data

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Demographic Data
Relation to Proband proband
Sex Male
 
Data Elements
Clinical Element Type: Duchenne Muscular Dystrophy
  (Baseline)
Diagnosis
Age at Diagnosis (in years)  8
Age at first symptom or medical concern  1
Relative with similar muscle disease  Yes
If yes, give their relationship(s) to you  BROTHER
Skeletal/Mobility
Scoliosis  Unknown
Broken bones due to DMD  No
Delays in motor development was initially recognized  Yes
Toe Walking initially recognized  Unknown
Enlarged calves initially recognized  Unknown
Walking  Yes
If yes, type of walking device  NONE AS YET
Mobility device ie stroller, wheelchair  No
Stand without aid  Yes
Sit without aid  Yes
Neurologic
Problem controlling behavior  No
Learning disability  No
Treatment
Use of corticosteroids  Yes
If yes, list those you are currently taking  PREDNISONE
What is the current dosage of medication(s)  DAILY
Use of alternative therapies  No
Taking heart medication  Yes
Tendon release surgery  No
Laboratory Tests
Taken the Forced Vital Capacity (FVC%) test  No
Cardiomyopathy  No
Cardiac MRI  Yes
Echocardiogram  Yes
Holter monitor  Yes
Taken the Left Ventricular Fraction (LVEF) test  Unknown
Taken the Left Ventricular Shortening Fraction (LVSF) test  Unknown
Had muscle biopsy  Unknown
Molecular Tests
Genetic test performed  Yes
If yes, list identified mutation  DUPLICATION OF EXONS 3-44
Remarks Clinically affected; affected brother is GM23244; delayed motor development; frequent falls; diagnosed at 8 years of age; walks without assistance; currently on daily corticosteroids; also on Enalapril; donor subject has a duplication of exons 3-44 in the DMD gene

External Links

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Gene Cards DMD
Gene Ontology GO:0003779 actin binding
GO:0005200 structural constituent of cytoskeleton
GO:0005509 calcium ion binding
GO:0005856 cytoskeleton
GO:0006936 muscle contraction
GO:0007016 cytoskeletal anchoring
GO:0007517 muscle development
GO:0008270 zinc ion binding
GO:0016010 dystrophin-associated glycoprotein complex
NCBI Gene Gene ID:1756
NCBI GTR 300377 DYSTROPHIN; DMD
310200 MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD
OMIM 300377 DYSTROPHIN; DMD
310200 MUSCULAR DYSTROPHY, DUCHENNE TYPE; DMD
Omim Description APO-DYSTROPHIN 1, INCLUDED
  BMDDYSTROPHIN, INCLUDED; DMD, INCLUDED
  CARDIOMYOPATHY, X-LINKED DILATED, INCLUDED; XLCM, INCLUDED
  MUSCULAR DYSTROPHY, PSEUDOHYPERTROPHIC PROGRESSIVE, DUCHENNE AND BECKERTYPES; DMD

Culture Protocols

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Split Ratio 1:4
Temperature 37 C
Percent CO2 5%
Percent O2 AMBIENT
Medium Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Not Inactivated
Substrate None specified
Subcultivation Method dilution - add fresh medium
Supplement -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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